Papers: 10.1186/s12859-021-04060-4

https://doi.org/10.1186/s12859-021-04060-4

Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers

Cited by: 6
Author(s): Pierre‐Julien Viailly, Vincent Sater, Mathieu Viennot, Élodie Bohers, Nicolas Vergne, Caroline Bérard, Hélène Dauchel, Thierry Lecroq, Alison Celebi, Philippe Ruminy, Vinciane Marchand, Marie‐Delphine Lanic, Sydney Dubois, Dominique Penther, Hervé Tilly, Sylvain Mareschal, Fabrice Jardin
Published: over 5 years ago

Software Mentions 2

bioconductor: Rsamtools
Binary alignment (BAM), FASTA, variant call (BCF), and tabix file import
Papers that mentioned: 138
Very Likely Science (90)
cran: cghRA
Array CGH Data Analysis and Visualization
Papers that mentioned: 1
Very Likely Science (60)